Antidiabetic activity and molecular docking of fructooligosaccharides produced by Aureobasidium pullulans in poloxamer-407-induced T2DM rats

被引:27
作者
Bharti, Sudhanshu Kumar [1 ]
Krishnan, Supriya [2 ]
Kumar, Amit [3 ]
Rajak, Kaushal Kishore [4 ]
Murari, Krishna [5 ]
Bharti, Binod Kumar [5 ]
Gupta, Ashok Kumar [1 ,6 ]
机构
[1] Univ Patna, Dept Biochem, Patna 800005, Bihar, India
[2] Banaras Hindu Univ, Dept Psychol, Varanasi 221005, Uttar Pradesh, India
[3] Jawaharlal Nehru Univ, Sch Computat & Integrat Sci, New Delhi 110067, India
[4] Indian Vet Res Inst, Dept Virol, Naini Tal 263138, Uttarakhand, India
[5] Bihar Agr Univ, Sanjay Gandhi Inst Dairy Technol, Patna 800014, Bihar, India
[6] Natl Inst Pharmaceut Educ & Res, Dept Biotechnol, Hajipur 844101, Bihar, India
关键词
Fructooligosaccharides; Diabetes mellitus; Molecular docking; DPP-IV inhibitor; Peroxisome proliferator-activated receptor-gamma agonists; HEPATIC GLUCOSE-PRODUCTION; LIPID-METABOLISM; OLIGOSACCHARIDES; INHIBITION; VALIDATION; MECHANISMS; PARAMETERS; FIBERS; INULIN;
D O I
10.1016/j.foodchem.2012.08.083
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This study evaluated the beneficial effects of fructooligosaccharide (FOS) intake from Aureobasidium pullulans using poloxamer-407 (PX-407) induced type 2 diabetes mellitus (T2DM) in rat. Administration of FOS enhanced enzymatic activities of catalase and glutathione reductase in a dose-dependent manner. Significant reduction in fasting plasma triacylglycerol and very low-density lipoprotein level coupled with slight increase in fasting plasma insulin level was observed. Significant decrease in severe glucosuria, proteinuria, blood creatinine, urea and advanced glycation end products was also observed. Supplementation of FOS increased glucagon like peptide-1 content as well as Bifidobacteria and Lactobacilli populations in the caecum. Molecular docking by Gold and Glide software revealed that three sugar types present in the FOS (1-kestose, nystose, and 1-beta-fructofuranosyl nystose) are potent dipeptidyl peptidase-IV inhibitors as well as peroxisome proliferator-activated receptor-gamma agonists. This work indicates that FOS can be positioned as a nutraceutical product, beneficial in diabetes-associated metabolic abnormalities. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:813 / 821
页数:9
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